Search results

Search for "supramolecular interactions" in Full Text gives 52 result(s) in Beilstein Journal of Organic Chemistry.

Gold extraction at the molecular level using α- and β-cyclodextrins

  • Susana Santos Braga

Beilstein J. Org. Chem. 2025, 21, 1116–1125, doi:10.3762/bjoc.21.89

Graphical Abstract
  • Susana Santos Braga LAQV-REQUIMTE and Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal 10.3762/bjoc.21.89 Abstract Cyclodextrins (CDs) are known for their ability to form supramolecular interactions with a wide range of guest molecules. In this review, focus is given on
  • spontaneous complex formation between α-CD and tetrabromoaurate and its current status of use in a few mining sites in the United States. Keywords: bromoaurate; cyanoaurate; cyclodextrin inclusion; self-assembly; supramolecular interactions; Introduction Gold has allured and captivated humankind ever since
PDF
Album
Review
Published 06 Jun 2025

Active-metal template clipping synthesis of novel [2]rotaxanes

  • Cătălin C. Anghel,
  • Teodor A. Cucuiet,
  • Niculina D. Hădade and
  • Ion Grosu

Beilstein J. Org. Chem. 2023, 19, 1776–1784, doi:10.3762/bjoc.19.130

Graphical Abstract
  • presence of supramolecular interactions that pre-organize rotaxane’s components is crucial for an efficient synthesis. The precursors of rotaxanes are supramolecular architectures held together by numerous interactions leading to diverse motifs such as ammonium crown ether (ion-dipole, hydrogen bonding
  • MIMs. This approach is a proof of concept which will be further developed along with improvements in the design of the supramolecular interactions between the axle station(s) and macrocycle components in order to provide an important alternative method in rotaxane synthesis. Experimental General
PDF
Album
Supp Info
Full Research Paper
Published 20 Nov 2023

Synthesis of ether lipids: natural compounds and analogues

  • Marco Antônio G. B. Gomes,
  • Alicia Bauduin,
  • Chloé Le Roux,
  • Romain Fouinneteau,
  • Wilfried Berthe,
  • Mathieu Berchel,
  • Hélène Couthon and
  • Paul-Alain Jaffrès

Beilstein J. Org. Chem. 2023, 19, 1299–1369, doi:10.3762/bjoc.19.96

Graphical Abstract
  • with biomembranes via supramolecular interactions with the lipids and proteins that are embedded in these membranes. We can hypothesis that their mechanism of action occurs via a direct interaction with membrane proteins or by a modification of the biophysical properties of the membranes. It must be
PDF
Album
Review
Published 08 Sep 2023

Light-responsive rotaxane-based materials: inducing motion in the solid state

  • Adrian Saura-Sanmartin

Beilstein J. Org. Chem. 2023, 19, 873–880, doi:10.3762/bjoc.19.64

Graphical Abstract
  • pseudorotaxanes, the supramolecular interactions between the counterparts are retained, thus constituting stable intertwined species showing analogous properties to those of rotaxanes. The pseudorotaxanes 1 were constituted by a dibenzo-24-crown-8 cyclic component and an ammonium-based thread functionalized with
PDF
Album
Perspective
Published 14 Jun 2023

In-depth characterization of self-healing polymers based on π–π interactions

  • Josefine Meurer,
  • Julian Hniopek,
  • Johannes Ahner,
  • Michael Schmitt,
  • Jürgen Popp,
  • Stefan Zechel,
  • Kalina Peneva and
  • Martin D. Hager

Beilstein J. Org. Chem. 2021, 17, 2496–2504, doi:10.3762/bjoc.17.166

Graphical Abstract
  • mechanical behavior was studied using rheology. The activation of the supramolecular interactions results in a breaking of these noncovalent bonds, which was investigated using IR spectroscopy, leading to a sufficient increase in mobility and, finally, a healing of the mechanical damage. This scratch-healing
  • were synthesized and characterized in detail. The mechanical and thermal behavior was studied revealing an activation of the supramolecular interactions at 125 °C. This finding could also be verified by temperature-depending IR-spectroscopy indicating a broadening of the aromatic signals at 150 °C
PDF
Album
Supp Info
Full Research Paper
Published 29 Sep 2021

Halides as versatile anions in asymmetric anion-binding organocatalysis

  • Lukas Schifferer,
  • Martin Stinglhamer,
  • Kirandeep Kaur and
  • Olga García Macheño

Beilstein J. Org. Chem. 2021, 17, 2270–2286, doi:10.3762/bjoc.17.145

Graphical Abstract
  • a field. Thus, the use of the halide in the catalyst–anion complex as both a mere counter-anion spectator or an active nucleophile has been depicted, along with the new trends toward additional noncovalent contacts within the HB-donor catalyst and supramolecular interactions to both the anion and
PDF
Album
Review
Published 01 Sep 2021

Constrained thermoresponsive polymers – new insights into fundamentals and applications

  • Patricia Flemming,
  • Alexander S. Münch,
  • Andreas Fery and
  • Petra Uhlmann

Beilstein J. Org. Chem. 2021, 17, 2123–2163, doi:10.3762/bjoc.17.138

Graphical Abstract
  • detail. According to the type of supramolecular interactions governing the thermoresponsive behavior UCST type polymers can be classified into two categories. Although various molecular forces such as van der Waals interactions and hydrophobic effects contribute to the thermoresponsiveness of polymers
PDF
Album
Review
Published 20 Aug 2021

Insight into functionalized-macrocycles-guided supramolecular photocatalysis

  • Minzan Zuo,
  • Krishnasamy Velmurugan,
  • Kaiya Wang,
  • Xueqi Tian and
  • Xiao-Yu Hu

Beilstein J. Org. Chem. 2021, 17, 139–155, doi:10.3762/bjoc.17.15

Graphical Abstract
  • occupancy 95%) in MeOH/H2O solutions (0.25:0.75, 0.5:0.5, and 0:1, respectively). This may be due to fact that the CD-functionalized sensitizing group could increase the product yield through excited-state supramolecular interactions within the cavity. In addition, the spacer attached to the primary hydroxy
PDF
Album
Review
Published 18 Jan 2021

Supramolecular polymers with reversed viscosity/temperature profile for application in motor oils

  • Jan-Erik Ostwaldt,
  • Christoph Hirschhäuser,
  • Stefan K. Maier,
  • Carsten Schmuck and
  • Jochen Niemeyer

Beilstein J. Org. Chem. 2021, 17, 105–114, doi:10.3762/bjoc.17.11

Graphical Abstract
  • -complementary [14] binding units (BU, blue) and a connecting linker unit (LU, green) to connect the BUs. In this case, the BUs are ureidopyrimidone units, which dimerize due to a fourfold hydrogen bond, thus allowing for strong supramolecular interactions [15]. Due to the flexibility of the LUs, the BUs can
  • transformation is occurring. Next to the system described by Sijbesma and Meijer, other compounds have been described that influence the viscosity by dynamic supramolecular interactions, also leading to a viscosity increase at elevated temperatures [16][17][18]. Inspired by these pioneering works of Sijbesma and
  • ). This led to the identification of one final candidate that was successfully applied as a VII in two motor oils, which is unprecedented for a low-molecular weight VII. Results and Discussion Developing a VII system based on supramolecular interactions Based on our working hypothesis, a supramolecular
PDF
Album
Supp Info
Full Research Paper
Published 12 Jan 2021

Selective recognition of ATP by multivalent nano-assemblies of bisimidazolium amphiphiles through “turn-on” fluorescence response

  • Rakesh Biswas,
  • Surya Ghosh,
  • Shubhra Kanti Bhaumik and
  • Supratim Banerjee

Beilstein J. Org. Chem. 2020, 16, 2728–2738, doi:10.3762/bjoc.16.223

Graphical Abstract
  • . One of the challenges in the bio-anion detection is that the sensory probes have to be effective under physiological conditions. The highly polar nature of the aqueous media considerably weakens supramolecular interactions such as H-bonding and electrostatic interactions and as a result, it is in
PDF
Album
Supp Info
Full Research Paper
Published 10 Nov 2020

Particle size effect in the mechanically assisted synthesis of β-cyclodextrin mesitylene sulfonate

  • Stéphane Menuel,
  • Sébastien Saitzek,
  • Eric Monflier and
  • Frédéric Hapiot

Beilstein J. Org. Chem. 2020, 16, 2598–2606, doi:10.3762/bjoc.16.211

Graphical Abstract
  • bioavailability [11][12][13]. In our previous studies, CDs acted either as reactants [14][15], or as additives [16][17], and were shown to display supramolecular interactions with the other reaction partners. We demonstrated that the formation of CD/substrate supramolecular complexes favored the dispersion of the
PDF
Album
Supp Info
Full Research Paper
Published 22 Oct 2020

1,2,3-Triazolium macrocycles in supramolecular chemistry

  • Mastaneh Safarnejad Shad,
  • Pulikkal Veettil Santhini and
  • Wim Dehaen

Beilstein J. Org. Chem. 2019, 15, 2142–2155, doi:10.3762/bjoc.15.211

Graphical Abstract
  • groups due to the anion binding, including chloride and other oxoanion salts. They also proved that the anions binding strength falls in line with their basicity as seen in the series AcO− > H2PO4− > Cl− > SO42− >NO3−. 2.5. 1,2,3-Triazolium macrocycles and [2]rotaxanes Supramolecular interactions could
PDF
Album
Review
Published 12 Sep 2019

Reversible end-to-end assembly of selectively functionalized gold nanorods by light-responsive arylazopyrazole–cyclodextrin interaction

  • Maximilian Niehues,
  • Patricia Tegeder and
  • Bart Jan Ravoo

Beilstein J. Org. Chem. 2019, 15, 1407–1415, doi:10.3762/bjoc.15.140

Graphical Abstract
  • aggregates can be realized more or less efficiently through various approaches based on supramolecular interactions like metal–metal and π–π interactions [11], DNA mediated [12] or by host–guest chemistry [13]. Most of these approaches require selective functionalization of the ends of the AuNR and take
PDF
Album
Supp Info
Full Research Paper
Published 26 Jun 2019

Aqueous olefin metathesis: recent developments and applications

  • Valerio Sabatino and
  • Thomas R. Ward

Beilstein J. Org. Chem. 2019, 15, 445–468, doi:10.3762/bjoc.15.39

Graphical Abstract
  • possesses one of the highest non-covalent binding affinities (Kd = 10−12–10−15 M). This exceptional affinity warrants the ArM remaining assembled throughout catalysis. Biotinylated HG-type catalysts anchored within (strept)avidin through supramolecular interactions were tested in the RCM of N,N
  • -Chymotrypsin interacts with catalyst 66 through supramolecular interactions followed by covalent nucleophilic attack to afford ArM 3. Assembling an artificial metathase (ArM 4) based on the small heat shock protein from M. Jannaschii (MjHSP). The protein structure is based on the atomic coordinates in PDB
PDF
Album
Review
Published 14 Feb 2019

LCST phase behavior of benzo-21-crown-7 with different alkyl chains

  • Yan Deng,
  • Xing Li,
  • Qiao Zhang,
  • Zheng Luo,
  • Chengyou Han and
  • Shengyi Dong

Beilstein J. Org. Chem. 2019, 15, 437–444, doi:10.3762/bjoc.15.38

Graphical Abstract
  • molecules-containing systems has been developed exhibiting LCST behavior and adjustable thermo-responsive properties. These include ionic liquids [27][28][29][30], macrocycles [31][32][33][34], and supramolecular pairs [26][35][36][37][38]. For example, the combination of macrocycles and supramolecular
  • interactions can realize controlled release and product separation in complex supramolecular systems [35]. More options of small molecules with LCST properties not only give rise to more flexibility for LCST systems and thermo-responsive materials, but would be a great advantage for functionalization. In our
PDF
Album
Supp Info
Letter
Published 14 Feb 2019

Olefin metathesis catalysts embedded in β-barrel proteins: creating artificial metalloproteins for olefin metathesis

  • Daniel F. Sauer,
  • Johannes Schiffels,
  • Takashi Hayashi,
  • Ulrich Schwaneberg and
  • Jun Okuda

Beilstein J. Org. Chem. 2018, 14, 2861–2871, doi:10.3762/bjoc.14.265

Graphical Abstract
  • are supramolecular, dative and covalent anchoring. Supramolecular anchoring was pioneered by Wilson and Whitesides in 1978 [27]. They made use of the high affinity of (strept)avidin (Sav) to biotin that represents one of the strongest supramolecular interactions found in nature with a dissociation
PDF
Album
Review
Published 19 Nov 2018

Calixazulenes: azulene-based calixarene analogues – an overview and recent supramolecular complexation studies

  • Paris E. Georghiou,
  • Shofiur Rahman,
  • Abdullah Alodhayb,
  • Hidetaka Nishimura,
  • Jaehyun Lee,
  • Atsushi Wakamiya and
  • Lawrence T. Scott

Beilstein J. Org. Chem. 2018, 14, 2488–2494, doi:10.3762/bjoc.14.225

Graphical Abstract
  • between the azulene rings and the C60, “edge-to-face” type interactions with the 2′,6′-protons of the phenyl group substituents of the azulenes are also factors which could stabilize the solid-state supramolecular interactions or complexation. In the present study, however, due to the dilute solution
PDF
Album
Supp Info
Full Research Paper
Published 25 Sep 2018

An uracil-linked hydroxyflavone probe for the recognition of ATP

  • Márton Bojtár,
  • Péter Zoltán Janzsó-Berend,
  • Dávid Mester,
  • Dóra Hessz,
  • Mihály Kállay,
  • Miklós Kubinyi and
  • István Bitter

Beilstein J. Org. Chem. 2018, 14, 747–755, doi:10.3762/bjoc.14.63

Graphical Abstract
  • ratiometric fluorescent nature. First, we examined the possible structure and the supramolecular interactions by quantum chemical calculations of our target compound, UHF (uracil-hydroxyflavone) and ATP (see Figure 1 for structures). The theoretical results indicated the possibility of base-pairing
PDF
Album
Supp Info
Full Research Paper
Published 03 Apr 2018

Binding abilities of polyaminocyclodextrins: polarimetric investigations and biological assays

  • Marco Russo,
  • Daniele La Corte,
  • Annalisa Pisciotta,
  • Serena Riela,
  • Rosa Alduina and
  • Paolo Lo Meo

Beilstein J. Org. Chem. 2017, 13, 2751–2763, doi:10.3762/bjoc.13.271

Graphical Abstract
  • to the fact that, once again, simple polarimetry proves to be a versatile and powerful tool for the study of supramolecular interactions, even in situations where quite complex systems are involved. Experimental Materials All the reagents needed were used as purchased (Sigma, Aldrich), without
PDF
Album
Supp Info
Full Research Paper
Published 18 Dec 2017

Binding abilities of a chiral calix[4]resorcinarene: a polarimetric investigation on a complex case of study

  • Marco Russo and
  • Paolo Lo Meo

Beilstein J. Org. Chem. 2017, 13, 2698–2709, doi:10.3762/bjoc.13.268

Graphical Abstract
  • interactions, π–π interactions, desolvation effects and entropy-unfavorable conformational dynamic restraints. Polarimetry is confirmed as a very useful and versatile tool for the investigation of supramolecular interactions with chiral hosts, even in complex systems involving multiple equilibria. Keywords
PDF
Album
Supp Info
Full Research Paper
Published 15 Dec 2017

Novel approach to hydroxy-group-containing porous organic polymers from bisphenol A

  • Tao Wang,
  • Yan-Chao Zhao,
  • Li-Min Zhang,
  • Yi Cui,
  • Chang-Shan Zhang and
  • Bao-Hang Han

Beilstein J. Org. Chem. 2017, 13, 2131–2137, doi:10.3762/bjoc.13.211

Graphical Abstract
  • that are enhanced by weak supramolecular interactions with C–H atoms on the aromatic rings of the polymers [38]. The isosteric heat of adsorption for carbon dioxide is calculated from adsorption data collected at 273 and 298 K using a virial method and the Clausius–Clapeyron equation [39] (Supporting
PDF
Album
Supp Info
Full Research Paper
Published 12 Oct 2017

Interactions between shape-persistent macromolecules as probed by AFM

  • Johanna Blass,
  • Jessica Brunke,
  • Franziska Emmerich,
  • Cédric Przybylski,
  • Vasil M. Garamus,
  • Artem Feoktystov,
  • Roland Bennewitz,
  • Gerhard Wenz and
  • Marcel Albrecht

Beilstein J. Org. Chem. 2017, 13, 938–951, doi:10.3762/bjoc.13.95

Graphical Abstract
  • persistent macromolecules with high structural rigidity are able to form stable aggregates based on multiple supramolecular interactions, which can be detected and quantified without the presence of side effects, such as self-passivation or coiling processes. Dendrimers, nanoparticles and shape-persistent
  • polyconjugated polymers ranged from 6 to 16 nm, depending on the side groups and the method of determination [9][10][11]. Among many supramolecular interactions, such as hydrogen bonding, π–π-interactions or hydrophobic host–guest interactions [12][13][14][15][16], the interactions of cyclodextrins (CDs) with
  • investigation of cooperativity of multiple host–guest interactions using AFM has been reported by several groups [40][41][42][43][44][45]. Huskens and co-workers measured the supramolecular interactions between a β-CD-modified planar surface and mono-, di- and trivalent adamantane guest molecules attached to an
PDF
Album
Supp Info
Full Research Paper
Published 18 May 2017

NMR reaction monitoring in flow synthesis

  • M. Victoria Gomez and
  • Antonio de la Hoz

Beilstein J. Org. Chem. 2017, 13, 285–300, doi:10.3762/bjoc.13.31

Graphical Abstract
  • [20]. Despite these disadvantages, interesting applications of planar microcoils can be found in literature. Hence, Velders et al. [25] studied supramolecular interactions by 19F NMR spectroscopy at the picomole level. This application takes advantage of the high sensitivity and large chemical-shift
PDF
Album
Review
Published 14 Feb 2017

Interactions between photoacidic 3-hydroxynaphtho[1,2-b]quinolizinium and cucurbit[7]uril: Influence on acidity in the ground and excited state

  • Jonas Becher,
  • Daria V. Berdnikova,
  • Darinka Dzubiel,
  • Heiko Ihmels and
  • Phil M. Pithan

Beilstein J. Org. Chem. 2017, 13, 203–212, doi:10.3762/bjoc.13.23

Graphical Abstract
  • derivatives may be modulated by supramolecular interactions. Considering the ability of this class of compounds to operate as DNA-binding ligands [56] or water-soluble chemosensors [57], we anticipate that the combination of these properties with the potential for modulation by host–guest assembly may widen
PDF
Album
Supp Info
Full Research Paper
Published 01 Feb 2017

Supramolecular frameworks based on [60]fullerene hexakisadducts

  • Andreas Kraft,
  • Johannes Stangl,
  • Ana-Maria Krause,
  • Klaus Müller-Buschbaum and
  • Florian Beuerle

Beilstein J. Org. Chem. 2017, 13, 1–9, doi:10.3762/bjoc.13.1

Graphical Abstract
  • stabilities and metal-free synthesis, but in most cases, have the disadvantages of poor crystallinity and limited processability or solution-phase characterization. In contrast, the formation of robust porous structures by means of supramolecular interactions between rigid organic molecules might be a
  • tested other polar solvents for crystallization in order to strengthen the supramolecular interactions that hold the networks together. For both C3 and C4, we could finally grow single crystals suitable for X-ray diffraction by slow vapor deposition of Et2O into EtOH solutions of both fullerene
PDF
Album
Supp Info
Full Research Paper
Published 02 Jan 2017
Other Beilstein-Institut Open Science Activities